P24055
1-Phenyl-1,2-ethanediol
97%
Sinónimos:
(±)-1-Phenyl-1,2-ethanediol, (±)-Phenylethylene glycol
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Fórmula lineal:
C6H5CH(OH)CH2OH
Número CAS:
Peso molecular:
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-258-1
Beilstein/REAXYS Number:
1306723
MDL number:
Assay:
97%
Form:
solid
Servicio técnico
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97%
form
solid
bp
272-274 °C/760 mmHg (lit.)
mp
66-68 °C (lit.)
SMILES string
OCC(O)c1ccccc1
InChI
1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2
InChI key
PWMWNFMRSKOCEY-UHFFFAOYSA-N
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ashwini C Mathpati et al.
Journal of biotechnology, 262, 1-10 (2017-09-30)
Kinetic resolution of rac-1,2-diols using the biocatalyst Burkholderia cepacia lipase (BCL) immobilized on a biodegradable binary blend support of hydroxypropyl methyl cellulose(HPMC)/polyvinyl alcohol (PVA) has been investigated. The immobilization technique improved enzyme activity significantly and it has excellent recyclability with
Yao Nie et al.
Organic & biomolecular chemistry, 9(11), 4070-4078 (2011-04-21)
The application of biocatalysis to the synthesis of chiral molecules is one of the greenest technologies for the replacement of chemical routes due to its environmentally benign reaction conditions and unparalleled chemo-, regio- and stereoselectivities. We have been interested in
Yanbin Liu et al.
Journal of industrial microbiology & biotechnology, 33(4), 274-282 (2005-12-02)
A microorganism with the ability to catalyze the resolution of racemic phenyloxirane was isolated and identified as Aspergillus niger SQ-6. Chiral capillary electrophoresis was successfully applied to separate both phenyloxirane and phenylethanediol. The epoxide hydrolase (EH) involved in this resolution